Human iPS cell-derived cartilaginous tissue spatially and functionally replaces nucleus pulposus
Human iPS cell-derived cartilaginous tissue spatially and functionally replaces nucleus pulposus
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人类iPS细胞衍生的软骨组织在空间和功能上替代髓核
DOI:
10.1016/j.biomaterials.2022.121491
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发表时间:
2022-04-05
期刊:
影响因子:
14
通讯作者:
Tsumaki, Noriyuki
中科院分区:
文献类型:
--
作者:
Kamatani, Takashi;Hagizawa, Hiroki;Tsumaki, Noriyuki
The loss of nucleus pulposus (NP) precedes the intervertebral disk (IVD) degeneration that causes back pain. Here, we demonstrate that the implantation of human iPS cell-derived cartilaginous tissue (hiPS-Cart) restores this loss by replacing lost NP spatially and functionally. NP cells consist of notochordal NP cells and chondrocyte-like NP cells. Single cell RNA sequencing (scRNA-seq) analysis revealed that cells in hiPS-Cart corresponded to chondrocyte-like NP cells but not to notochordal NP cells. The implantation of hiPS-Cart into a nuclectomized space of IVD in nude rats prevented the degeneration of the IVD and preserved its mechanical properties. hiPS-Cart survived and occupied the nuclectomized space for at least six months after implantation, indicating spatial and functional replacement of lost NP by hiPS-Cart. Further scRNA-seq analysis revealed that hiPS-Cart cells changed their profile after implantation, differentiating into two lineages that are metabolically distinct from each other. However, post-implanted hiPS-Cart cells corresponded to chondrocyte-like NP cells only and did not develop into notochordal NP cells, suggesting that chondrocyte-like NP cells are nearly sufficient for NP function. The data collectively indicate that hiPS-Cart is a candidate implant for regenerating NP spatially and functionally and preventing IVD degeneration.